TAK-147, an acetylcholinesterase inhibitor, increases choline acetyltransferase activity in cultured rat septal cholinergic neurons

TAK-147, a potent acetylcholinesterase (AChE) inhibitor, potentiated choline acetyltransferase (ChAT) activity in cultured rat septal cholinergic neurons in a concentration-dependent manner with an EC 50 value of 4.47 nM. Donepezil, another potent AChE inhibitor, also increased ChAT activity althoug...

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Veröffentlicht in:Neuroscience letters 1999-01, Vol.260 (1), p.5-8
Hauptverfasser: Kato, Koki, Hayako, Hitomi, Ishihara, Yuji, Marui, Shogo, Iwane, Makoto, Miyamoto, Masaomi
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Sprache:eng
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Zusammenfassung:TAK-147, a potent acetylcholinesterase (AChE) inhibitor, potentiated choline acetyltransferase (ChAT) activity in cultured rat septal cholinergic neurons in a concentration-dependent manner with an EC 50 value of 4.47 nM. Donepezil, another potent AChE inhibitor, also increased ChAT activity although its potency was less than that of TAK-147. Other AChE inhibitors (rivastigmine, tacrine, physostigmine and neostigmine) showed no effect. The effects of TAK-147 were greater in the presence of NGF, suggesting a synergistic action of TAK-147 and NGF. TAK-147 and donepezil showed high affinity for σ receptors, whereas tacrine and physostigmine did not. Haloperidol and ifenprodil, high-affinity σ ligands, potently enhanced ChAT activity in the septal neurons. These results suggest that TAK-147 may have neurotrophic activity on central cholinergic neurons, not via AChE inhibition but possibly via an effect on σ receptors.
ISSN:0304-3940
1872-7972
DOI:10.1016/S0304-3940(98)00943-4